Canonical Allele Identifier: PA2828048832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2500Ile
CA014137
NM_001354904.2:c.7499C>T