Canonical Allele Identifier: PA2826801281
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3402
ClinVar RCV Id: RCV000003571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Phe479Ser
CA116187
NM_001291594.2:c.1436T>C