Allele Registry

Canonical Allele Identifier: PA3057469815

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV005004834

ClinVar Variation:

3574325

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Gln215Glu	CA1267162 NM_014625.4:c.643C>G