Canonical Allele Identifier: PA2827968655
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 657857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1655Glu
CA040478
NM_001354898.2:c.4963C>G