Canonical Allele Identifier: PA2827681475
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 179186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ala566Thr
CA183904
NM_001352777.2:c.1696G>A