Allele Registry

Canonical Allele Identifier: PA2828913862

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018402

RCV001553652

ClinVar Variation:

16903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369591.2:p.Cys516Tyr	CA257655 NM_001382662.3:c.1547G>A