Canonical Allele Identifier: PA2828013856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg88Gln
CA007680
NM_001354903.2:c.263G>A