Canonical Allele Identifier: PA2827998951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala2525Thr
CA049041
NM_001354901.2:c.7573G>A