Allele Registry

Canonical Allele Identifier: PA2829759087

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV004527185

ClinVar Variation:

3233905

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Arg196Gly	CA1267178 NM_014625.4:c.586C>G