Canonical Allele Identifier: PA2827680612
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 964094
ClinVar RCV Id: RCV001238242 RCV002402748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ala571Thr
CA399493004
NM_001352776.2:c.1711G>A