Allele Registry

Canonical Allele Identifier: PA096958

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

71147

ClinVar RCV:

RCV000049921

ClinVar Variation:

56508

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Ile171Asn	CA250245 NM_004646.4:c.512T>A