Allele Registry

Canonical Allele Identifier: PA2828913871

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018411

ClinVar Variation:

16911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369591.2:p.Tyr525Cys	CA257665 NM_001382662.3:c.1574A>G