Canonical Allele Identifier: PA2828023028
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630899
ClinVar Variation Id: 1047386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1395Glu
CA16032340
NM_001354906.2:c.4184G>A
CA1573473273
NM_001354906.2:c.4184_4185delinsAA