Canonical Allele Identifier: PA2827947058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys2357Glu
CA16036732
NM_001354895.2:c.7069A>G