Canonical Allele Identifier: PA2827949854
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2102478
ClinVar RCV Id: RCV003744899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile404Val
CA16023953
NM_001354896.2:c.1210A>G