Canonical Allele Identifier: PA2828011959
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758666
ClinVar RCV Id: RCV002380462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2373Thr
CA16037427
NM_001354902.2:c.7117T>A