Canonical Allele Identifier: PA350829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 221081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg876Gln
CA032826
NM_001127510.3:c.2627G>A