Canonical Allele Identifier: PA2828912486
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 256840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Ala500Val
CA4304165
NM_001382657.2:c.1499C>T