Canonical Allele Identifier: PA2573280768
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1392740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Pro587Leu
CA8565140
NM_021991.4:c.1760C>T