Canonical Allele Identifier: PA2827679765
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1392740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Pro587Leu
CA8565140
NM_001352775.2:c.1760C>T