Canonical Allele Identifier: PA2828016041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr279Met
CA005437
NM_001354906.2:c.836C>T