Canonical Allele Identifier: PA2827679672
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1376508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Ala509Ser
CA399494084
NM_001352775.2:c.1525G>T