Canonical Allele Identifier: PA2827677435
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 3222009
ClinVar RCV Id: RCV004513427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Ser77Pro
CA399506034
NM_001352773.2:c.229T>C