Canonical Allele Identifier: PA2828002106
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His1284Arg
CA037682
NM_001354902.2:c.3851A>G