Canonical Allele Identifier: PA2827677950
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2056662
ClinVar RCV Id: RCV002922956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ala522dup
CA983781376
NM_001352773.2:c.1563_1565dup