Canonical Allele Identifier: PA2827948561
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2813Lys
CA16039637
NM_001354895.2:c.8438C>A