Canonical Allele Identifier: PA2826801138
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 289888
ClinVar RCV Id: RCV000334924 RCV000861203 RCV001102311 RCV001102312 RCV001354108 RCV002518104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Ser328Asn
CA554073
NM_001291594.2:c.983G>A