Allele Registry

Canonical Allele Identifier: PA2827680927

Gene: JUP HGNC NCBI

ClinVar Variation Id: 468751

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Gly92Asp	CA8565526 NM_001352777.2:c.275G>A