Allele Registry

Canonical Allele Identifier: PA2827679027

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV001938115

ClinVar Variation:

1408671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339703.1:p.Thr700Ile	CA399490769 NM_001352774.2:c.2099C>T