Canonical Allele Identifier: PA2827680931
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201809
ClinVar RCV Id: RCV000183483 RCV001798638 RCV001047557 RCV001192707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Glu96Lys
CA308451
NM_001352777.2:c.286G>A