Allele Registry

Canonical Allele Identifier: PA658826366

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV003965420

ClinVar Variation:

545635

HGVS (amino-acid)	Matching Registered Transcripts
NP_000761.3:p.Arg139Lys	CA5617795 NM_000770.3:c.416G>A