Canonical Allele Identifier: PA2827979962
Gene: APC HGNC NCBI
ClinVar Allele:
1812580
ClinVar RCV:
RCV002378177
ClinVar Variation:
1756402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2298Gly
CA16036540
NM_001354899.2:c.6892C>G