Canonical Allele Identifier: PA2827677953
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 409989
ClinVar RCV Id: RCV000475805 RCV000618384 RCV001799663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ala522Val
CA16615357
NM_001352773.2:c.1565C>T