Canonical Allele Identifier: PA2828014756
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg230His
CA012635
NM_001354903.2:c.689G>A