Allele Registry

Canonical Allele Identifier: PA097021

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000049865

ClinVar Variation:

56452

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Leu610Gln	CA250146 NM_004646.4:c.1829T>A