Canonical Allele Identifier: PA2827677536
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1450398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ala162Ser
CA399503612
NM_001352773.2:c.484G>T