Canonical Allele Identifier: PA2741857521
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688895
ClinVar RCV Id: RCV003490660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001323.1:p.Pro220Ser
CA359282149
NM_001332.4:c.658C>T