Canonical Allele Identifier: PA2828044601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1867Arg
CA16034419
NM_001354904.2:c.5600C>G