Canonical Allele Identifier: PA2827998196
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2297Ala
CA046771
NM_001354901.2:c.6889A>G