Canonical Allele Identifier: PA2828015099
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg131His
CA004108
NM_001354906.2:c.392G>A