Allele Registry

Canonical Allele Identifier: PA3057469825

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV005004800

ClinVar Variation:

3574218

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Arg322Gly	CA343565703 NM_014625.4:c.964C>G