Canonical Allele Identifier: PA2827678021
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2950055
ClinVar RCV Id: RCV003807413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ile580Phe
CA399492875
NM_001352773.2:c.1738A>T