Canonical Allele Identifier: PA2827680590
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2177943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Gln548Glu
CA8565174
NM_001352776.2:c.1642C>G