Allele Registry

Canonical Allele Identifier: PA2828912289

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018405

ClinVar Variation:

16906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369586.2:p.Tyr178Asp	CA257660 NM_001382657.2:c.532T>G