Canonical Allele Identifier: PA2828027775
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly2269Val
CA046963
NM_001354903.2:c.6806G>T