Allele Registry

Canonical Allele Identifier: PA3057469801

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV005008925

ClinVar Variation:

3574446

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Gly35Val	CA343553832 NM_014625.4:c.104G>T