Canonical Allele Identifier: PA2826800509
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3402
ClinVar RCV Id: RCV000003571
JSON-LD

Amino-acid Alleles

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