Canonical Allele Identifier: PA2828028576
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2231Ala
CA048361
NM_001354906.2:c.6691A>G