Canonical Allele Identifier: PA2826225030
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079524
ClinVar RCV Id: RCV004367918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185783.1:p.Gly337Glu
CA377677559
NM_001198854.1:c.1010G>A