Allele Registry

Canonical Allele Identifier: PA2826841967

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000005697

ClinVar Variation:

5366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Gly92Cys	CA117454 NM_001297575.2:c.274G>T