Canonical Allele Identifier: PA2828027657
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2096Pro
CA16036870
NM_001354906.2:c.6286A>C