Canonical Allele Identifier: PA645399053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly907Arg
CA033124
NM_001127510.3:c.2719G>A
CA033134
NM_001127510.3:c.2719G>C