Canonical Allele Identifier: PA297659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala928Thr
CA007787
NM_000038.6:c.2782G>A