Canonical Allele Identifier: PA2828019113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411437
ClinVar RCV Id: RCV002230525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gln934Pro
CA16028133
NM_001354903.2:c.2801A>C