Canonical Allele Identifier: PA2827346502
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078696
ClinVar RCV Id: RCV004374985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Asp242Glu
CA359281861
NM_001332.4:c.726C>G
CA359281862
NM_001332.4:c.726C>A