Canonical Allele Identifier: PA2827948113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2698335
ClinVar RCV Id: RCV003536165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2676Pro
CA16038762
NM_001354895.2:c.8026A>C