Canonical Allele Identifier: PA2827971293
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2456Ile
CA16037529
NM_001354898.2:c.7367C>T