Canonical Allele Identifier: PA2828010798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2106_Ser2110del
CA16042098
NM_001354905.2:c.6316_6330del