Canonical Allele Identifier: PA2827951066
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730223
ClinVar RCV Id: RCV002326403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1126Ile
CA16028622
NM_001354896.2:c.3377A>T