Allele Registry

Canonical Allele Identifier: PA913198585

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000783660

RCV001770046

ClinVar Variation:

39352

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Arg144His	CA5616437 NM_000769.4:c.431G>A