Canonical Allele Identifier: PA2825013811
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln264Arg
CA049479
NM_000038.6:c.791A>G