Allele Registry

Canonical Allele Identifier: PA2828913018

Gene: POR HGNC NCBI

ClinVar RCV:

RCV000018412

ClinVar Variation:

16912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369587.2:p.[Leu609_Asp612del;Glu614_Trp617del]	CA257667 NM_001382658.3:c.1826_1849del