The invention relates to the field of
molecular biology, and discloses a method for detecting
gene mutation of
human cytochrome P450 CYP2C19, which comprises the following steps of: performing amplification on a sample
genome by using primers, wherein the primers comprise upstream and downstream primers for detecting M1
mutation, and upstream and downstream primers for detecting M2
mutation, the nucleotides of the upstream and downstream primers for detecting M1 mutation are shown as SEQ ID No.1 and SEQ ID No.2, and the nucleotides of the upstream and downstream primers for detecting M2 mutation are shown as SEQ ID No.5 and SEQ ID No.6; and setting a reference for
quality control, and sequencing an amplification product by using sequencing primers of which the nucleotides are shown as SEQ ID No.9 and SEQ ID No.10. The invention also provides a kit for detecting
gene mutation of
human cytochrome P450 CYP2C19. According to detection results of the method, guidance and adjustment of clinical medication schemes are carried out, a basis is provided for clinical individualized medication, the
treatment effect can be improved and the toxic and
side effect risks can be reduced.