Canonical Allele Identifier: PA2828047980
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2388Ala
CA048361
NM_001354904.2:c.7162A>G