Allele Registry

Canonical Allele Identifier: PA2827679190

Gene: JUP HGNC NCBI

ClinVar Variation Id: 468751

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339704.1:p.Gly92Asp	CA8565526 NM_001352775.2:c.275G>A