Canonical Allele Identifier: PA2827980811
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676783
ClinVar RCV Id: RCV003470242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2557Glu
CA16038170
NM_001354899.2:c.7669A>G