Allele Registry

Canonical Allele Identifier: PA658826367

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV000656545

RCV003980283

ClinVar Variation:

545585

HGVS (amino-acid)	Matching Registered Transcripts
NP_000761.3:p.Ile264Met	CA5617661 NM_000770.3:c.792C>G