Allele Registry

Canonical Allele Identifier: PA2827681572

Gene: JUP HGNC NCBI

ClinVar Variation Id: 179306

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Ala645Thr	CA184163 NM_001352777.2:c.1933G>A