Allele Registry

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Canonical Allele Identifier: PA2826713340

Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078696

ClinVar RCV Id: RCV004374985

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001275644.1:p.Asp151Glu	CA359281861 NM_001288715.1:c.453C>G CA359281862 NM_001288715.1:c.453C>A