Canonical Allele Identifier: PA2829777846
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1977132
ClinVar RCV Id: RCV002750622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Ser1358Phe
CA553364
NM_015102.5:c.4073C>T