Canonical Allele Identifier: PA2825252870
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079516
ClinVar RCV Id: RCV004367910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000760.1:p.Asp414His
CA377675129
NM_000769.4:c.1240G>C