Canonical Allele Identifier: PA2829369040
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1777987
ClinVar RCV Id: RCV002414566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Gly562Asp
CA399493150
NM_002230.4:c.1685G>A