Canonical Allele Identifier: PA2828913426
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369588.2:p.Cys566Tyr
CA257655
NM_001382659.3:c.1697G>A