Canonical Allele Identifier: PA2827980940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2598Ile
CA014137
NM_001354899.2:c.7793C>T