Canonical Allele Identifier: PA2828030701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2712Lys
CA16039637
NM_001354903.2:c.8135C>A