Canonical Allele Identifier: PA2827980122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2351Ile
CA10582339
NM_001354899.2:c.7052C>T