Allele Registry

Canonical Allele Identifier: PA658826368

Gene: CYP2C8 HGNC NCBI

ClinVar RCV:

RCV000656546

ClinVar Variation:

545586

HGVS (amino-acid)	Matching Registered Transcripts
NP_000761.3:p.Ile269Phe	CA5617657 NM_000770.3:c.805A>T