Allele Registry

Canonical Allele Identifier: PA2828913436

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018411

ClinVar Variation:

16911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369588.2:p.Tyr575Cys	CA257665 NM_001382659.3:c.1724A>G