Canonical Allele Identifier: PA916017821
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 501425
ClinVar RCV Id: RCV000778988 RCV000595557 RCV001055295 RCV001074439 RCV001335698 RCV002476329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Thr610Pro
CA553638
NM_001291594.2:c.1828A>C