Canonical Allele Identifier: PA2827678177
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2926646
ClinVar RCV Id: RCV003788884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Pro713Leu
CA8565000
NM_001352773.2:c.2138C>T