Canonical Allele Identifier: PA2827679767
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2933113
ClinVar RCV Id: RCV003790231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Leu588Val
CA399492786
NM_001352775.2:c.1762C>G