Canonical Allele Identifier: PA2827679039
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1786311
ClinVar RCV Id: RCV002417688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Val709Met
CA399490672
NM_001352774.2:c.2125G>A