Allele Registry

Canonical Allele Identifier: PA2828913181

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018405

ClinVar Variation:

16906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369588.2:p.Tyr178Asp	CA257660 NM_001382659.3:c.532T>G