Canonical Allele Identifier: PA2827968643
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg1651Gly
CA009838
NM_001354898.2:c.4951A>G
CA2740097766
NM_001354898.2:c.4951_4959delinsGGAGGAGGA