Canonical Allele Identifier: PA645402036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2379Ile
CA10582339
NM_001127510.3:c.7136C>T