Canonical Allele Identifier: PA2827974892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg777Gln
CA031897
NM_001354899.2:c.2330G>A