Canonical Allele Identifier: PA2828913477
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 284175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369588.2:p.Val628Ile
CA4304330
NM_001382659.3:c.1882G>A