Canonical Allele Identifier: PA2827984565
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774878
ClinVar RCV Id: RCV003586060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser929_Asp930delinsAsn
CA2697546210
NM_001354900.2:c.2786_2788del