Allele Registry

Canonical Allele Identifier: PA658676202

Gene: POR HGNC NCBI

ClinVar Variation Id: 2040336

HGVS (amino-acid)	Matching Registered Transcripts
NP_000932.3:p.Phe72Leu	CA4303514 NM_000941.3:c.214T>C CA367747177 NM_000941.3:c.216T>A CA367747179 NM_000941.3:c.216T>G