Canonical Allele Identifier: PA2827942331
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala928Thr
CA007787
NM_001354895.2:c.2782G>A