Allele Registry

Canonical Allele Identifier: PA095467

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000005699

RCV000516417

RCV001273616

ClinVar Variation:

5368

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Val180Met	CA117458 NM_014625.4:c.538G>A