Canonical Allele Identifier: PA645399107
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411437
ClinVar RCV Id: RCV002230525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln1035Pro
CA16028133
NM_001127510.3:c.3104A>C