Canonical Allele Identifier: PA2828031097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg74Trp
CA007948
NM_001354904.2:c.220C>T