Allele Registry

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Canonical Allele Identifier: PA2826713321

Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688898

ClinVar RCV Id: RCV003490663

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001275644.1:p.Glu126Asp	CA359282224 NM_001288715.1:c.378G>T CA359282225 NM_001288715.1:c.378G>C