Canonical Allele Identifier: PA2827681469
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1777987
ClinVar RCV Id: RCV002414566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Gly562Asp
CA399493150
NM_001352777.2:c.1685G>A