Canonical Allele Identifier: PA2827681477
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201827
ClinVar RCV Id: RCV000183503 RCV002399671 RCV002517815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ile569Phe
CA308546
NM_001352777.2:c.1705A>T