Canonical Allele Identifier: PA2827981069
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 962583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Cys2636Arg
CA16038686
NM_001354899.2:c.7906T>C