Canonical Allele Identifier: PA2828019691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1015Asp
CA008298
NM_001354903.2:c.3044G>A