Canonical Allele Identifier: PA2826713364
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078698
ClinVar RCV Id: RCV004374987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Gly234Asp
CA359281355
NM_001288715.1:c.701G>A