Canonical Allele Identifier: PA916042357
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg99Gln
CA007959
NM_001354903.2:c.296G>A