Canonical Allele Identifier: PA2827681501
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2938903
ClinVar RCV Id: RCV003791629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Pro587Ser
CA399492793
NM_001352777.2:c.1759C>T