Canonical Allele Identifier: PA126962
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 16898
ClinVar RCV Id: RCV000018396 RCV000348667 RCV000783657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000760.1:p.Arg433Trp
CA126961
NM_000769.4:c.1297C>T