Canonical Allele Identifier: PA2827678028
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1392740
ClinVar RCV Id: RCV001912383 RCV002407012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Pro587Leu
CA8565140
NM_001352773.2:c.1760C>T