Canonical Allele Identifier: PA2827984351
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly866Arg
CA033124
NM_001354900.2:c.2596G>A
CA033134
NM_001354900.2:c.2596G>C