Canonical Allele Identifier: PA2828048518
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala2458Thr
CA049041
NM_001354904.2:c.7372G>A