Allele Registry

Canonical Allele Identifier: PA2573216007

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018403

ClinVar Variation:

16904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369584.2:p.Val623Phe	CA257657 NM_001382655.3:c.1867G>T