Canonical Allele Identifier: PA2827982822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg355His
CA004108
NM_001354900.2:c.1064G>A