Canonical Allele Identifier: PA2828023265
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630899
ClinVar Variation Id: 1047386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1577Glu
CA16032340
NM_001354903.2:c.4730G>A
CA1573473273
NM_001354903.2:c.4730_4731delinsAA