Canonical Allele Identifier: PA2829369005
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 571627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Arg540Cys
CA8565182
NM_002230.4:c.1618C>T