Canonical Allele Identifier: PA2826713323
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2348805
ClinVar RCV Id: RCV002956565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Ala128Val
CA114394868
NM_001288715.1:c.383C>T