Canonical Allele Identifier: PA2827678309
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1403658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Arg84Gly
CA399505898
NM_001352774.2:c.250C>G