Canonical Allele Identifier: PA2826225108
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079524
ClinVar RCV Id: RCV004367918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185784.1:p.Gly369Glu
CA377677559
NM_001198855.1:c.1106G>A