Canonical Allele Identifier: PA2828028839
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760034
ClinVar RCV Id: RCV002396452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His2271Asn
CA16037972
NM_001354906.2:c.6811C>A