Canonical Allele Identifier: PA2828131072
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444649
ClinVar RCV Id: RCV000512866 RCV003493615
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351057.1:p.Gln170Pro
CA3200842
NM_001364128.2:c.509A>C