Canonical Allele Identifier: PA2827962501
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676783
ClinVar RCV Id: RCV003470242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2595Glu
CA16038170
NM_001354897.2:c.7783A>G