Canonical Allele Identifier: PA2828007336
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774878
ClinVar RCV Id: RCV003586060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser879_Asp880delinsAsn
CA2697546210
NM_001354902.2:c.2636_2638del