Canonical Allele Identifier: PA2827973401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg274Gln
CA16023293
NM_001354899.2:c.821G>A