Canonical Allele Identifier: PA2826800822
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431959
ClinVar RCV Id: RCV001941020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278522.1:p.Ala820Gly
CA338049325
NM_001291593.2:c.2459C>G