Allele Registry

Canonical Allele Identifier: PA2826841892

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000409834

RCV003574266

ClinVar Variation:

370679

2771430

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Met1Ile