Canonical Allele Identifier: PA2827985031
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1075Asp
CA008298
NM_001354900.2:c.3224G>A