Canonical Allele Identifier: PA2829368386
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 536636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Val232Ile
CA8565412
NM_002230.4:c.694G>A