Canonical Allele Identifier: PA2827972324
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala2770Thr
CA015437
NM_001354898.2:c.8308G>A