Canonical Allele Identifier: PA2828022351
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Lys1442Glu
CA10578378
NM_001354903.2:c.4324A>G