Canonical Allele Identifier: PA087790
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 222661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Met193Thr
CA087549
NM_021991.4:c.578T>C