Allele Registry

Canonical Allele Identifier: PA645375300

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000361967

RCV001125721

RCV001272299

RCV003417918

ClinVar Variation:

290122

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Ser220Ala	CA9390706 NM_004646.4:c.658T>G