Canonical Allele Identifier: PA2827980790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062362
ClinVar RCV Id: RCV003771188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2551Gly
CA16038130
NM_001354899.2:c.7652A>G