Canonical Allele Identifier: PA2827678882
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2143679
ClinVar RCV Id: RCV003068005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Asp573Tyr
CA290696004
NM_001352774.2:c.1717G>T