Canonical Allele Identifier: PA2827998889
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760169
ClinVar RCV Id: RCV002400545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2507Ile
CA16038051
NM_001354901.2:c.7520G>T