Canonical Allele Identifier: PA2825252891
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079524
ClinVar RCV Id: RCV004367918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000761.3:p.Gly439Glu
CA377677559
NM_000770.3:c.1316G>A