Canonical Allele Identifier: PA2828027658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2096Ile
CA10582339
NM_001354906.2:c.6287C>T