Canonical Allele Identifier: PA2825637644
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774671
ClinVar RCV Id: RCV003585861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser275Thr
CA16023238
NM_001127511.3:c.824G>C