Allele Registry

Canonical Allele Identifier: PA2827677504

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV000688130

ClinVar Variation:

567920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339702.1:p.Asp136Tyr	CA399505019 NM_001352773.2:c.406G>T