Canonical Allele Identifier: PA2827966497
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469907
ClinVar RCV Id: RCV003742670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1009Val
CA16028127
NM_001354898.2:c.3026A>T