Canonical Allele Identifier: PA2827681671
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 958279
ClinVar RCV Id: RCV001231418 RCV002429986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Asp731Asn
CA8564990
NM_001352777.2:c.2191G>A