Canonical Allele Identifier: PA2827678319
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2942872
ClinVar RCV Id: RCV003808038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Met89Lys
CA399505773
NM_001352774.2:c.266T>A