Canonical Allele Identifier: PA2828028827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2269Cys
CA16037960
NM_001354906.2:c.6805A>T