Canonical Allele Identifier: PA2825019249
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1193Arg
CA16029193
NM_000038.6:c.3578A>G