Canonical Allele Identifier: PA2827980577
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566948
ClinVar RCV Id: RCV003278260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2485Arg
CA16037718
NM_001354899.2:c.7454C>G