Canonical Allele Identifier: PA2827985096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1092Glu
CA16028782
NM_001354900.2:c.3276T>A
CA16028783
NM_001354900.2:c.3276T>G