Canonical Allele Identifier: PA2829245707
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001382342.1:p.Cys566Tyr
CA257655
NM_001395413.1:c.1697G>A