Canonical Allele Identifier: PA168073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg405Gln
CA004099
NM_000038.6:c.1214G>A