Canonical Allele Identifier: PA2827680829
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1719394
ClinVar RCV Id: RCV002303692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Gln17Lys
CA399507207
NM_001352777.2:c.49C>A