Canonical Allele Identifier: PA2827679909
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2165875
ClinVar RCV Id: RCV003090203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Pro710His
CA399490658
NM_001352775.2:c.2129C>A