Allele Registry

Canonical Allele Identifier: PA2828913377

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000251974

RCV000405449

RCV001292550

RCV001640493

ClinVar Variation:

256840

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369588.2:p.Ala500Val	CA4304165 NM_001382659.3:c.1499C>T