Allele Registry

Canonical Allele Identifier: PA2828913805

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018400

ClinVar Variation:

16901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369591.2:p.Val439Glu	CA257651 NM_001382662.3:c.1316T>A