Allele Registry

Canonical Allele Identifier: PA2827678696

Gene: JUP HGNC NCBI

ClinVar Variation Id: 409988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339703.1:p.Leu408Phe	CA8565250 NM_001352774.2:c.1222C>T