Allele Registry

Canonical Allele Identifier: PA2826225021

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV002508783

RCV003970100

ClinVar Variation:

375654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185783.1:p.Lys297Arg	CA5617527 NM_001198854.1:c.890A>G CA658832940 NM_001198854.1:c.[890A>G;110G>A]