Canonical Allele Identifier: PA2828017064
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2779708
ClinVar RCV Id: RCV003745664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys455Glu
CA16026178
NM_001354906.2:c.1363A>G