Canonical Allele Identifier: PA2829777811
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380519
ClinVar RCV Id: RCV001886383 RCV002490103
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Ala1340Thr
CA17124873
NM_015102.5:c.4018G>A