Allele Registry

Canonical Allele Identifier: PA2828912990

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018411

ClinVar Variation:

16911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369587.2:p.Tyr575Cys	CA257665 NM_001382658.3:c.1724A>G