Allele Registry

Canonical Allele Identifier: PA2826224912

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV003965420

ClinVar Variation:

545635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185782.1:p.Arg69Lys	CA5617795 NM_001198853.1:c.206G>A