Canonical Allele Identifier: PA2826713328
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1241651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Pro135dup
CA443542024
NM_001288715.1:c.404_406dup
CA2592214785
NM_001288715.1:c.395_396insCCC