Canonical Allele Identifier: PA2827979963
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2298Gln
CA012730
NM_001354899.2:c.6893G>A