Canonical Allele Identifier: PA2827980236
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2384Glu
CA16037088
NM_001354899.2:c.7150A>G