Canonical Allele Identifier: PA2827680597
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 239104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Met556Thr
CA8565152
NM_001352776.2:c.1667T>C