Canonical Allele Identifier: PA2827681470
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1401540
ClinVar RCV Id: RCV001912927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Cys563Tyr
CA8565151
NM_001352777.2:c.1688G>A