Canonical Allele Identifier: PA2827681676
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1915991
ClinVar RCV Id: RCV002594246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Pro735Ser
CA399490325
NM_001352777.2:c.2203C>T