Canonical Allele Identifier: PA2827976066
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1118Cys
CA035367
NM_001354899.2:c.3352C>T