Canonical Allele Identifier: PA2827681483
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Arg572Gln
CA8565145
NM_001352777.2:c.1715G>A