Canonical Allele Identifier: PA2827678305
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 855054
ClinVar RCV Id: RCV001060226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Thr78Ala
CA399506016
NM_001352774.2:c.232A>G