Canonical Allele Identifier: PA2828009377
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1873Glu
CA010908
NM_001354905.2:c.5619C>G
CA16034682
NM_001354905.2:c.5619C>A