Canonical Allele Identifier: PA2828032033
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gln239Arg
CA049479
NM_001354904.2:c.716A>G