Canonical Allele Identifier: PA2827989659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1485763
ClinVar RCV Id: RCV003745494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2473Asn
CA16037722
NM_001354900.2:c.7418C>A