Canonical Allele Identifier: PA2580201287
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2348805
ClinVar RCV Id: RCV002956565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Ala219Val
CA114394868
NM_001332.4:c.656C>T