Canonical Allele Identifier: PA2827989203
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2338Ile
CA10582339
NM_001354900.2:c.7013C>T