Canonical Allele Identifier: PA2828011492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 860089
ClinVar RCV Id: RCV003649376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2214Cys
CA16036839
NM_001354905.2:c.6640A>T