Canonical Allele Identifier: PA2828913031
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 284175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Val628Ile
CA4304330
NM_001382658.3:c.1882G>A