Canonical Allele Identifier: PA2741842099
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2559398
ClinVar RCV Id: RCV004329684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185784.1:p.Ile71Thr
CA377682933
NM_001198855.1:c.212T>C