Allele Registry

Canonical Allele Identifier: PA2826225002

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV000656546

ClinVar Variation:

545586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185783.1:p.Ile167Phe	CA5617657 NM_001198854.1:c.499A>T