Canonical Allele Identifier: PA916017042
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444649
ClinVar RCV Id: RCV000512866 RCV003493615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275646.1:p.Gln74Pro
CA3200842
NM_001288717.2:c.221A>C