Canonical Allele Identifier: PA2827940161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg230His
CA012635
NM_001354895.2:c.689G>A