Canonical Allele Identifier: PA2827681445
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 917779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Arg540His
CA8565181
NM_001352777.2:c.1619G>A