Allele Registry

Canonical Allele Identifier: PA097157

Gene: NPHP4 HGNC NCBI

ClinVar RCV:

RCV000003571

ClinVar Variation:

3402

HGVS (amino-acid)	Matching Registered Transcripts
NP_055917.1:p.Phe991Ser	CA116187 NM_015102.5:c.2972T>C