Allele Registry

Canonical Allele Identifier: PA2826842004

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000005691

RCV000414576

RCV001003814

RCV001171338

RCV001275640

RCV001328321

RCV003944802

ClinVar Variation:

5360

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Arg138Gln	CA117446 NM_001297575.2:c.413G>A