Canonical Allele Identifier: PA916041319
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2397Pro
CA16036870
NM_001354896.2:c.7189A>C