Canonical Allele Identifier: PA2827681181
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2563202
ClinVar RCV Id: RCV003301363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Leu294Phe
CA399500643
NM_001352777.2:c.880C>T