Canonical Allele Identifier: PA2829777821
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1986817
ClinVar RCV Id: RCV002805611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Glu1342Lys
CA338049205
NM_015102.5:c.4024G>A