Canonical Allele Identifier: PA2827947108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 860089
ClinVar RCV Id: RCV003649376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2374Cys
CA16036839
NM_001354895.2:c.7120A>T