Canonical Allele Identifier: PA2827679675
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2222075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Pro512Ala
CA399494054
NM_001352775.2:c.1534C>G