Canonical Allele Identifier: PA2827678198
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 958279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Asp731Asn
CA8564990
NM_001352773.2:c.2191G>A