Allele Registry

Canonical Allele Identifier: PA2826224943

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV000656545

RCV003980283

ClinVar Variation:

545585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185782.1:p.Ile194Met	CA5617661 NM_001198853.1:c.582C>G