Allele Registry

Canonical Allele Identifier: PA346573

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000157401

RCV002498780

RCV002515049

RCV002516361

ClinVar Variation:

180465

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Gly958Glu	CA346571 NM_004646.4:c.2873G>A