Allele Registry

Canonical Allele Identifier: PA2828913895

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018403

ClinVar Variation:

16904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369591.2:p.Val555Phe	CA257657 NM_001382662.3:c.1663G>T