Canonical Allele Identifier: PA2825023572
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2266_Ser2270del
CA16042098
NM_000038.6:c.6796_6810del