Canonical Allele Identifier: PA2827986891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1635Gly
CA009838
NM_001354900.2:c.4903A>G
CA2740097766
NM_001354900.2:c.4903_4911delinsGGAGGAGGA