Allele Registry

Canonical Allele Identifier: PA2827681590

Gene: JUP HGNC NCBI

ClinVar Allele:

401992

ClinVar RCV:

RCV000757415

RCV001079037

RCV001127665

RCV001127666

RCV002418404

ClinVar Variation:

409985

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Arg661Gln	CA8565056 NM_001352777.2:c.1982G>A