Canonical Allele Identifier: PA2826801058
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 194764
ClinVar RCV Id: RCV000175205 RCV000204681 RCV000392070 RCV001573161 RCV002294061 RCV001093856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Asp241Asn
CA334827
NM_001291594.2:c.721G>A