Canonical Allele Identifier: PA2827681486
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 323168
ClinVar RCV Id: RCV000303926 RCV000397661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Asp573Val
CA10650099
NM_001352777.2:c.1718A>T