Canonical Allele Identifier: PA2828027815
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2278Ile
CA10582339
NM_001354903.2:c.6833C>T