Canonical Allele Identifier: PA2827995468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1465Arg
CA339419
NM_001354901.2:c.4394T>G