Canonical Allele Identifier: PA2827346527
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_001323.1:p.Gly325Asp
CA359281355
NM_001332.4:c.974G>A