Canonical Allele Identifier: PA2828018692
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774878
ClinVar RCV Id: RCV003586060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser869_Asp870delinsAsn
CA2697546210
NM_001354903.2:c.2606_2608del