Allele Registry

Canonical Allele Identifier: PA2828912568

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018403

ClinVar Variation:

16904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369586.2:p.Val605Phe	CA257657 NM_001382657.2:c.1813G>T