Allele Registry

Canonical Allele Identifier: PA2826225001

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV000656545

RCV003980283

ClinVar Variation:

545585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185783.1:p.Ile162Met	CA5617661 NM_001198854.1:c.486C>G