Allele Registry

Canonical Allele Identifier: PA2826842047

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000210051

ClinVar Variation:

224482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284504.1:p.Pro203Leu	CA354121 NM_001297575.2:c.608C>T