Canonical Allele Identifier: PA2827999087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2842780
ClinVar RCV Id: RCV003652433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2568Tyr
CA16038453
NM_001354901.2:c.7703C>A