Canonical Allele Identifier: PA2828048705
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2485Lys
CA049276
NM_001354904.2:c.7454C>A