Allele Registry

Canonical Allele Identifier: PA2827681092

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV001365790

ClinVar Variation:

1056895

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Glu217Gly	CA399502660 NM_001352777.2:c.650A>G