Allele Registry

Canonical Allele Identifier: PA645413419

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV002508783

RCV003970100

ClinVar Variation:

375654

HGVS (amino-acid)	Matching Registered Transcripts
NP_000761.3:p.Lys399Arg	CA5617527 NM_000770.3:c.1196A>G CA658832940 NM_000770.3:c.[1196A>G;416G>A]