Canonical Allele Identifier: PA916041581
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2626Thr
CA10582340
NM_001354896.2:c.7876G>A