Canonical Allele Identifier: PA2828042192
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630899
ClinVar Variation Id: 1047386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1552Glu
CA16032340
NM_001354904.2:c.4655G>A
CA1573473273
NM_001354904.2:c.4655_4656delinsAA