Canonical Allele Identifier: PA2827679917
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1786652
ClinVar RCV Id: RCV002430617
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Met716Val
CA399490578
NM_001352775.2:c.2146A>G