Allele Registry

Canonical Allele Identifier: PA096967

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

71150

ClinVar RCV:

RCV000049924

ClinVar Variation:

56511

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Ile173Asn	CA250251 NM_004646.4:c.518T>A