Canonical Allele Identifier: PA2826713368
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2510805
ClinVar RCV Id: RCV003240229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Val246Met
CA3200988
NM_001288715.1:c.736G>A