Allele Registry

Canonical Allele Identifier: PA096888

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

71082

ClinVar RCV:

RCV000049856

ClinVar Variation:

56443

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Cys528Phe	CA250127 NM_004646.4:c.1583G>T