Canonical Allele Identifier: PA2827678099
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 179306
ClinVar RCV Id: RCV000156095 RCV001850147 RCV004019870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ala645Thr
CA184163
NM_001352773.2:c.1933G>A