Canonical Allele Identifier: PA2827678405
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1517384
ClinVar RCV Id: RCV002027317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Ala163Thr
CA8565459
NM_001352774.2:c.487G>A