Canonical Allele Identifier: PA2827679449
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Gly298Ser
CA308501
NM_001352775.2:c.892G>A