Canonical Allele Identifier: PA2827991899
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg355His
CA004108
NM_001354901.2:c.1064G>A