Canonical Allele Identifier: PA2829245758
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 284175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001382342.1:p.Val628Ile
CA4304330
NM_001395413.1:c.1882G>A