Canonical Allele Identifier: PA645399919
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His1375Arg
CA037682
NM_001127510.3:c.4124A>G