Allele Registry

Canonical Allele Identifier: PA2828912139

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018412

ClinVar Variation:

16912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369584.2:p.[Leu627_Asp630del;Glu632_Trp635del]	CA257667 NM_001382655.3:c.1880_1903del