Canonical Allele Identifier: PA2829368136
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2054695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Ala80Thr
CA290700938
NM_002230.4:c.238G>A