Allele Registry

Canonical Allele Identifier: PA095370

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000208227

RCV000786958

RCV003556262

ClinVar Variation:

222762

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Pro118Leu	CA351864 NM_014625.4:c.353C>T