Canonical Allele Identifier: PA2826713335
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430945
ClinVar RCV Id: RCV000496061 RCV001755733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275644.1:p.Pro133Leu
CA114394865
NM_001288715.1:c.398C>T