Canonical Allele Identifier: PA2827346505
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078697
ClinVar RCV Id: RCV004374986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Ala250_Ala251del
CA2673260064
NM_001332.4:c.748_753del