Canonical Allele Identifier: PA2827992862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2779708
ClinVar RCV Id: RCV003745664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys679Glu
CA16026178
NM_001354901.2:c.2035A>G