Allele Registry

Canonical Allele Identifier: PA095144

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000005700

RCV000681927

RCV003352747

RCV003993738

ClinVar Variation:

5369

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Arg291Trp	CA117460 NM_014625.4:c.871C>T