Canonical Allele Identifier: PA2827992238
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr459Met
CA028394
NM_001354901.2:c.1376C>T