Allele Registry

Canonical Allele Identifier: PA2826842021

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000169326

RCV002515194

ClinVar Variation:

188952

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Arg168Cys	CA199102 NM_001297575.2:c.502C>T