Canonical Allele Identifier: PA2828912872
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 911635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Arg403His
CA4304027
NM_001382658.3:c.1208G>A