Allele Registry

Canonical Allele Identifier: PA2826800509

Gene: NPHP4 HGNC NCBI

ClinVar RCV:

RCV000003571

ClinVar Variation:

3402

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278522.1:p.Phe478Ser	CA116187 NM_001291593.2:c.1433T>C