Canonical Allele Identifier: PA2827998380
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys2353Glu
CA16037088
NM_001354901.2:c.7057A>G