Canonical Allele Identifier: PA2827980105
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met2345Arg
CA16036833
NM_001354899.2:c.7034T>G