Canonical Allele Identifier: PA2828016568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg370Met
CA16025598
NM_001354906.2:c.1109G>T