Allele Registry

Canonical Allele Identifier: PA126964

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000018397

RCV000018398

RCV000291495

RCV000783656

RCV002280093

ClinVar Variation:

16899

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Trp212Ter