Canonical Allele Identifier: PA2826801126
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 287002
ClinVar RCV Id: RCV000264657 RCV000868723 RCV003278741 RCV004543094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Arg308Trp
CA554114
NM_001291594.2:c.922C>T