Canonical Allele Identifier: PA2827973236
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp228Glu
CA16023011
NM_001354899.2:c.684T>A
CA16023012
NM_001354899.2:c.684T>G