Canonical Allele Identifier: PA2826713334
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316756
ClinVar RCV Id: RCV001769625 RCV002272494 RCV002540648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Pro130Leu
CA114394866
NM_001288715.1:c.389C>T