Canonical Allele Identifier: PA2827678873
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 892036
ClinVar RCV Id: RCV001127755 RCV001127754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Ile569Leu
CA399493029
NM_001352774.2:c.1705A>C