Canonical Allele Identifier: PA2828240747
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 911635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354491.2:p.Arg403His
CA4304027
NM_001367562.3:c.1208G>A