Canonical Allele Identifier: PA2827966772
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg1089Gln
CA035094
NM_001354898.2:c.3266G>A