Allele Registry

Canonical Allele Identifier: PA095168

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000005698

ClinVar Variation:

5367

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Asp160Gly	CA117456 NM_014625.4:c.479A>G