Canonical Allele Identifier: PA2827680814
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2448233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Thr739Ala
CA8564982
NM_001352776.2:c.2215A>G