Allele Registry

Canonical Allele Identifier: PA2826842014

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000735716

ClinVar Variation:

599118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Asp160Val	CA343568973 NM_001297575.2:c.479A>T