Canonical Allele Identifier: PA2828038564
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1149Thr
CA008695
NM_001354904.2:c.3446G>C