Canonical Allele Identifier: PA2827677443
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1403658
ClinVar RCV Id: RCV001909161 RCV003167082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Arg84Gly
CA399505898
NM_001352773.2:c.250C>G