Canonical Allele Identifier: PA2827992622
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3222645
ClinVar RCV Id: RCV004516030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His593Arg
CA029954
NM_001354901.2:c.1778A>G