Canonical Allele Identifier: PA2827680927
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Gly92Asp
CA8565526
NM_001352777.2:c.275G>A