Canonical Allele Identifier: PA2828047735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1449206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gln2354Glu
CA16037517
NM_001354904.2:c.7060C>G