Canonical Allele Identifier: PA2573215946
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 911635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369584.2:p.Arg421His
CA4304027
NM_001382655.3:c.1262G>A