Canonical Allele Identifier: PA2826224965
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050506
ClinVar RCV Id: RCV001358021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185783.1:p.Arg30Trp
CA5617800
NM_001198854.1:c.88C>T