Canonical Allele Identifier: PA2827952267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746373
ClinVar RCV Id: RCV002340960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln1769Arg
CA16032817
NM_001354896.2:c.5306A>G