Canonical Allele Identifier: PA2827944829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 657857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gln1680Glu
CA040478
NM_001354895.2:c.5038C>G