Canonical Allele Identifier: PA2825014170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg302Gln
CA16023293
NM_000038.6:c.905G>A