Allele Registry

Canonical Allele Identifier: PA645502525

Gene: NPHP4 HGNC NCBI

ClinVar Variation Id: 284756

HGVS (amino-acid)	Matching Registered Transcripts
NP_055917.1:p.Thr936Met	CA553929 NM_015102.5:c.2807C>T