Canonical Allele Identifier: PA2741857550
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2510805
ClinVar RCV Id: RCV003240229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Val337Met
CA3200988
NM_001332.4:c.1009G>A