Allele Registry

Canonical Allele Identifier: PA2827678529

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV001326823

ClinVar Variation:

1026386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339703.1:p.Glu258Gln	CA399501353 NM_001352774.2:c.772G>C