Canonical Allele Identifier: PA2828023435
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1601Glu
CA009865
NM_001354903.2:c.4802G>A