Allele Registry

Canonical Allele Identifier: PA2829245388

Gene: POR HGNC NCBI

ClinVar Variation Id: 469120

ClinVar Variation Id: 2040336

ClinVar RCV Id: RCV002912476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001382342.1:p.Phe69Leu	CA4303514 NM_001395413.1:c.205T>C CA367747177 NM_001395413.1:c.207T>A CA367747179 NM_001395413.1:c.207T>G