Allele Registry

Canonical Allele Identifier: PA913198582

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000782436

ClinVar Variation:

39350

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Arg132Gln	CA5616425 NM_000769.4:c.395G>A