Canonical Allele Identifier: PA2828021686
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1347Ile
CA16030848
NM_001354903.2:c.4040C>T