Canonical Allele Identifier: PA2828054935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly747Arg
CA033124
NM_001354905.2:c.2239G>A
CA033134
NM_001354905.2:c.2239G>C