Canonical Allele Identifier: PA916041489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2532Ala
CA048361
NM_001354896.2:c.7594A>G