Canonical Allele Identifier: PA2825641766
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1653Thr
CA16032296
NM_001127511.3:c.4957G>A