Canonical Allele Identifier: PA658660731
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470098
ClinVar RCV Id: RCV003537085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2528Val
CA16037809
NM_001127510.3:c.7582A>G