Canonical Allele Identifier: PA2828016001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566964
ClinVar RCV Id: RCV003306834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser269Pro
CA16024924
NM_001354906.2:c.805T>C