Canonical Allele Identifier: PA2827998564
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2409Pro
CA013665
NM_001354901.2:c.7225T>C