Canonical Allele Identifier: PA2827948951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg99Gln
CA007959
NM_001354896.2:c.296G>A