Canonical Allele Identifier: PA2827681004
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1742961
ClinVar RCV Id: RCV002330659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Val159Ala
CA399503649
NM_001352777.2:c.476T>C