Allele Registry

Canonical Allele Identifier: PA2573086187

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

1291636

ClinVar RCV:

RCV001733389

RCV002488494

ClinVar Variation:

1301353

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Gly412Ser	CA9390496 NM_004646.4:c.1234G>A