Canonical Allele Identifier: PA916042606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 143004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg97Gln
CA004061
NM_001354906.2:c.290G>A