Canonical Allele Identifier: PA2828912865
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 3064896
ClinVar RCV Id: RCV003989973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Glu395Ala
CA367749432
NM_001382658.3:c.1184A>C