Canonical Allele Identifier: PA2828913771
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 3064896
ClinVar RCV Id: RCV003989973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369591.2:p.Glu395Ala
CA367749432
NM_001382662.3:c.1184A>C