Canonical Allele Identifier: PA2827978003
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3014066
ClinVar RCV Id: RCV003875705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1703Val
CA16032680
NM_001354899.2:c.5108C>T