Canonical Allele Identifier: PA2828020205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His1109Tyr
CA008571
NM_001354903.2:c.3325C>T