Canonical Allele Identifier: PA2827998926
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760336
ClinVar RCV Id: RCV002400712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2518Thr
CA16038114
NM_001354901.2:c.7552T>A