Canonical Allele Identifier: PA2827679269
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2946944
ClinVar RCV Id: RCV003801134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Ala162Thr
CA399503615
NM_001352775.2:c.484G>A