Canonical Allele Identifier: PA2829369003
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 917779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Arg540His
CA8565181
NM_002230.4:c.1619G>A