Canonical Allele Identifier: PA2827998198
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys2298Glu
CA16036732
NM_001354901.2:c.6892A>G