Canonical Allele Identifier: PA2827999079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2567Ala
CA049327
NM_001354901.2:c.7699A>G