Canonical Allele Identifier: PA2827678871
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1778248
ClinVar RCV Id: RCV002414666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Ala566Gly
CA399493063
NM_001352774.2:c.1697C>G