Allele Registry

Canonical Allele Identifier: PA891849803

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV000688130

ClinVar Variation:

567920

HGVS (amino-acid)	Matching Registered Transcripts
NP_068831.1:p.Asp136Tyr	CA399505019 NM_021991.4:c.406G>T