Canonical Allele Identifier: PA2827681422
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2056662
ClinVar RCV Id: RCV002922956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ala522dup
CA983781376
NM_001352777.2:c.1563_1565dup