Canonical Allele Identifier: PA2580129895
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2283328
ClinVar RCV Id: RCV004138390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000760.1:p.His396Gln
CA377675018
NM_000769.4:c.1188T>A
CA377675019
NM_000769.4:c.1188T>G