Allele Registry

Canonical Allele Identifier: PA2828912980

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018402

RCV001553652

ClinVar Variation:

16903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369587.2:p.Cys566Tyr	CA257655 NM_001382658.3:c.1697G>A