Allele Registry

Canonical Allele Identifier: PA250056

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000018399

RCV000383294

RCV000782432

ClinVar Variation:

16900

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Met1Val