Allele Registry

Canonical Allele Identifier: PA2828913899

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018412

ClinVar Variation:

16912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369591.2:p.[Leu559_Asp562del;Glu564_Trp567del]	CA257667 NM_001382662.3:c.1676_1699del