Canonical Allele Identifier: PA2827983788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2779708
ClinVar RCV Id: RCV003745664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys697Glu
CA16026178
NM_001354900.2:c.2089A>G