Allele Registry

Canonical Allele Identifier: PA2827681549

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV000157252

RCV002408706

RCV002492607

ClinVar Variation:

180377

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Ala628Thr	CA346371 NM_001352777.2:c.1882G>A