Allele Registry

Canonical Allele Identifier: PA2828912477

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018400

ClinVar Variation:

16901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369586.2:p.Val489Glu	CA257651 NM_001382657.2:c.1466T>A