Allele Registry

Canonical Allele Identifier: PA2827681224

Gene: JUP HGNC NCBI

ClinVar RCV:

RCV001293223

ClinVar Variation:

978764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339706.1:p.Trp329Leu	CA399499469 NM_001352777.2:c.986G>T