Canonical Allele Identifier: PA2827950849
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1058Trp
CA008046
NM_001354896.2:c.3172A>T