Canonical Allele Identifier: PA2827951158
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1507413
ClinVar RCV Id: RCV003773388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu1154Gly
CA16028800
NM_001354896.2:c.3461A>G