Allele Registry

Canonical Allele Identifier: PA2826224969

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV003965420

ClinVar Variation:

545635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185783.1:p.Arg37Lys	CA5617795 NM_001198854.1:c.110G>A