Allele Registry

Canonical Allele Identifier: PA2826225103

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV002508783

RCV003970100

ClinVar Variation:

375654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185784.1:p.Lys329Arg	CA5617527 NM_001198855.1:c.986A>G CA658832940 NM_001198855.1:c.[986A>G;206G>A]