Allele Registry

Canonical Allele Identifier: PA2580238878

Gene: POR HGNC NCBI

ClinVar RCV:

RCV002975738

ClinVar Variation:

2071640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369584.2:p.Val623Ile	CA4304308 NM_001382655.3:c.1867G>A