Canonical Allele Identifier: PA645502470
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 297823
ClinVar RCV Id: RCV000340961 RCV000389927 RCV000523327 RCV000766889 RCV001257066 RCV002294254 RCV004537680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Glu399Gly
CA554598
NM_015102.5:c.1196A>G