Canonical Allele Identifier: PA2825014506
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp366Asn
CA026688
NM_000038.6:c.1096G>A