Canonical Allele Identifier: PA2827680769
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1061982
ClinVar RCV Id: RCV001371650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Pro703Arg
CA290694754
NM_001352776.2:c.2108C>G