Canonical Allele Identifier: PA2827990177
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761661
ClinVar RCV Id: RCV002419234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2631Ala
CA16038742
NM_001354900.2:c.7892G>C