Canonical Allele Identifier: PA2827680627
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 519077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Arg582Gln
CA290695975
NM_001352776.2:c.1745G>A