Canonical Allele Identifier: PA2827949889
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu422Lys
CA026951
NM_001354896.2:c.1264G>A