Canonical Allele Identifier: PA2827679055
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 860683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Met718Thr
CA8564996
NM_001352774.2:c.2153T>C