Canonical Allele Identifier: PA2828023015
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg1393Gly
CA009838
NM_001354906.2:c.4177A>G
CA2740097766
NM_001354906.2:c.4177_4185delinsGGAGGAGGA