Allele Registry

Canonical Allele Identifier: PA2573215897

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018405

ClinVar Variation:

16906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369584.2:p.Tyr196Asp	CA257660 NM_001382655.3:c.586T>G