Allele Registry

Canonical Allele Identifier: PA2827681318

Gene: JUP HGNC NCBI

ClinVar Variation Id: 409984

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Thr427Met	CA8565242 NM_001352777.2:c.1280C>T