Canonical Allele Identifier: PA2827679272
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1379750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Ala162Val
CA8565460
NM_001352775.2:c.485C>T