Canonical Allele Identifier: PA2827679190
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468751
ClinVar RCV Id: RCV000536647 RCV002289763 RCV002438426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Gly92Asp
CA8565526
NM_001352775.2:c.275G>A