Canonical Allele Identifier: PA2827680051
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 392175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Arg86Gln
CA8565535
NM_001352776.2:c.257G>A