Canonical Allele Identifier: PA2828011699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2288Ile
CA10582339
NM_001354902.2:c.6863C>T