Canonical Allele Identifier: PA2827959505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg1686Gly
CA009838
NM_001354897.2:c.5056A>G
CA2740097766
NM_001354897.2:c.5056_5064delinsGGAGGAGGA