Canonical Allele Identifier: PA2827677930
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468745
ClinVar RCV Id: RCV000551963 RCV000624487 RCV003235283 RCV001548482 RCV002395414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Gly503Ser
CA8565194
NM_001352773.2:c.1507G>A