Canonical Allele Identifier: PA2827679036
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2132265
ClinVar RCV Id: RCV003055992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Tyr705Phe
CA399490718
NM_001352774.2:c.2114A>T