Canonical Allele Identifier: PA916040230
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1468Gln
CA009471
NM_001354896.2:c.4403G>A