Allele Registry

Canonical Allele Identifier: PA645480934

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000394401

RCV000783659

ClinVar Variation:

39351

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Trp120Arg	CA5616409 NM_000769.4:c.358T>C CA377669877 NM_000769.4:c.358T>A