Allele Registry

Canonical Allele Identifier: PA097030

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

71116

ClinVar RCV:

RCV000049890

ClinVar Variation:

56477

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Leu832Pro	CA250193 NM_004646.4:c.2495T>C