Canonical Allele Identifier: PA2827972390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2788Lys
CA16039637
NM_001354898.2:c.8363C>A