Canonical Allele Identifier: PA916040488
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1694Gly
CA009838
NM_001354896.2:c.5080A>G
CA2740097766
NM_001354896.2:c.5080_5088delinsGGAGGAGGA