Canonical Allele Identifier: PA2827949874
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg414His
CA004108
NM_001354896.2:c.1241G>A