Allele Registry

Canonical Allele Identifier: PA913193461

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000735716

ClinVar Variation:

599118

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Asp160Val	CA343568973 NM_014625.4:c.479A>T