Canonical Allele Identifier: PA2826713345
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078697
ClinVar RCV Id: RCV004374986
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Ala159_Ala160del
CA2673260064
NM_001288715.1:c.475_480del