Allele Registry

Canonical Allele Identifier: PA2573215968

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018400

ClinVar Variation:

16901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369584.2:p.Val507Glu	CA257651 NM_001382655.3:c.1520T>A