Canonical Allele Identifier: PA2828021038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala1075Thr
CA008897
NM_001354906.2:c.3223G>A