Canonical Allele Identifier: PA2828027699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Lys2256Glu
CA16036732
NM_001354903.2:c.6766A>G