Canonical Allele Identifier: PA2828038694
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1166Met
CA008722
NM_001354904.2:c.3497C>T