Canonical Allele Identifier: PA2827980111
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1359860
ClinVar RCV Id: RCV003772508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2347Pro
CA16036847
NM_001354899.2:c.7040A>C