Canonical Allele Identifier: PA2827679191
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 449201
ClinVar RCV Id: RCV000524047 RCV000645198 RCV000617807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Gly92Cys
CA8565527
NM_001352775.2:c.274G>T