Canonical Allele Identifier: PA2827953263
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759762
ClinVar RCV Id: RCV002396180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu2552Gln
CA16037840
NM_001354896.2:c.7654G>C