Canonical Allele Identifier: PA2827999504
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185492
ClinVar Variation Id: 428124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu2691Lys
CA014471
NM_001354901.2:c.8070_8071delinsTA
CA16039228
NM_001354901.2:c.8071G>A