Canonical Allele Identifier: PA2828030138
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185492
ClinVar Variation Id: 428124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu2467Lys
CA014471
NM_001354906.2:c.7398_7399delinsTA
CA16039228
NM_001354906.2:c.7399G>A