Canonical Allele Identifier: PA2827680799
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1468213
ClinVar RCV Id: RCV001970604 RCV002425342 RCV003893030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ser730Gly
CA290694718
NM_001352776.2:c.2188A>G