Canonical Allele Identifier: PA1139699906
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 986194
ClinVar RCV Id: RCV001267480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Ala237Thr
CA359281921
NM_001332.4:c.709G>A