Canonical Allele Identifier: PA2828912417
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 2735034
ClinVar RCV Id: RCV003518763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Pro396_Glu398del
CA4304016
NM_001382657.2:c.1187_1195del