Canonical Allele Identifier: PA913198585
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 39352
ClinVar RCV Id: RCV000783660 RCV001770046
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Amino-acid Alleles

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