Canonical Allele Identifier: PA2828047241
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys2286Glu
CA16037088
NM_001354904.2:c.6856A>G