Allele Registry

Canonical Allele Identifier: PA2826841965

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV001933209

ClinVar Variation:

1415700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Gly92Ser	CA343552395 NM_001297575.2:c.274G>A