Canonical Allele Identifier: PA2741981192
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2563202
ClinVar RCV Id: RCV003301363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Leu294Phe
CA399500643
NM_021991.4:c.880C>T