Canonical Allele Identifier: PA2827950661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774878
ClinVar RCV Id: RCV003586060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser988_Asp989delinsAsn
CA2697546210
NM_001354896.2:c.2963_2965del