Canonical Allele Identifier: PA2828013135
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2466Ile
CA014137
NM_001354905.2:c.7397C>T