Canonical Allele Identifier: PA2827680998
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 449256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Glu154Lys
CA8565490
NM_001352777.2:c.460G>A