Canonical Allele Identifier: PA2828020774
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu1034Gln
CA008815
NM_001354906.2:c.3100G>C