Allele Registry

Canonical Allele Identifier: PA2828912567

Gene: POR HGNC NCBI

ClinVar RCV:

RCV002975738

ClinVar Variation:

2071640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369586.2:p.Val605Ile	CA4304308 NM_001382657.2:c.1813G>A