Canonical Allele Identifier: PA2827679397
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1026386
ClinVar RCV Id: RCV001326823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Glu258Gln
CA399501353
NM_001352775.2:c.772G>C