Canonical Allele Identifier: PA2828913913
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 284175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369591.2:p.Val578Ile
CA4304330
NM_001382662.3:c.1732G>A