Canonical Allele Identifier: PA2499249792
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1241651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Pro226dup
CA443542024
NM_001332.4:c.677_679dup
CA2592214785
NM_001332.4:c.668_669insCCC