Canonical Allele Identifier: PA2827940736
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg414His
CA004108
NM_001354895.2:c.1241G>A