Canonical Allele Identifier: PA2827988899
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2248Lys
CA16036318
NM_001354900.2:c.6743C>A