Canonical Allele Identifier: PA2825014812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu422Lys
CA026951
NM_000038.6:c.1264G>A