Canonical Allele Identifier: PA2827992556
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr567Ala
CA029787
NM_001354901.2:c.1699A>G