Canonical Allele Identifier: PA2828018618
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774878
ClinVar RCV Id: RCV003586060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser687_Asp688delinsAsn
CA2697546210
NM_001354906.2:c.2060_2062del