Canonical Allele Identifier: PA2827680762
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1785788
ClinVar RCV Id: RCV002424100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ala699Ser
CA8565005
NM_001352776.2:c.2095G>T