Allele Registry

Canonical Allele Identifier: PA645417279

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000409834

RCV003574266

ClinVar Variation:

370679

2771430

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Met1Ile