Canonical Allele Identifier: PA2826713322
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317661
ClinVar RCV Id: RCV001769668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Ala128Thr
CA114394869
NM_001288715.1:c.382G>A