Canonical Allele Identifier: PA2827680721
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 409985
ClinVar RCV Id: RCV000757415 RCV001079037 RCV001127665 RCV001127666 RCV002418404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Arg661Gln
CA8565056
NM_001352776.2:c.1982G>A