Allele Registry

Canonical Allele Identifier: PA2827681301

Gene: JUP HGNC NCBI

ClinVar Variation Id: 409988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Leu408Phe	CA8565250 NM_001352777.2:c.1222C>T