Canonical Allele Identifier: PA2825643965
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2361Ile
CA10582339
NM_001127511.3:c.7082C>T