Canonical Allele Identifier: PA2827680042
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2054695
ClinVar RCV Id: RCV002932907 RCV004067049 RCV004526211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ala80Thr
CA290700938
NM_001352776.2:c.238G>A