Canonical Allele Identifier: PA2829369041
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1401540
ClinVar RCV Id: RCV001912927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Cys563Tyr
CA8565151
NM_002230.4:c.1688G>A