Canonical Allele Identifier: PA2827998538
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1345335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Phe2403Ser
CA16037417
NM_001354901.2:c.7208T>C