Canonical Allele Identifier: PA2828006642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1720459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Glu1400Lys
CA16031584
NM_001354905.2:c.4198G>A