Canonical Allele Identifier: PA645460083
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 392175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Arg86Gln
CA8565535
NM_021991.4:c.257G>A