Canonical Allele Identifier: PA645399385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517
ClinVar RCV Id: RCV000571094 RCV002230588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1115Met
CA035105
NM_001127510.3:c.3343G>A