Canonical Allele Identifier: PA2828912358
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Ala284Pro
CA257653
NM_001382657.2:c.850G>C