Canonical Allele Identifier: PA2828022767
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570472
ClinVar RCV Id: RCV003534595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1347Ile
CA16032043
NM_001354906.2:c.4039G>A