Canonical Allele Identifier: PA297962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg109Gln
CA007959
NM_001127511.3:c.326G>A