Canonical Allele Identifier: PA2828031996
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp231Glu
CA16023011
NM_001354904.2:c.693T>A
CA16023012
NM_001354904.2:c.693T>G