Canonical Allele Identifier: PA2827678024
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 930073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Arg582Trp
CA8565142
NM_001352773.2:c.1744C>T