Canonical Allele Identifier: PA1139732928
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 928425
ClinVar RCV Id: RCV001192287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu996Arg
CA16028041
NM_001354898.2:c.2987T>G