Canonical Allele Identifier: PA2828028099
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2321Ala
CA012961
NM_001354903.2:c.6961A>G