Canonical Allele Identifier: PA2827998646
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759075
ClinVar RCV Id: RCV002391481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu2434Ile
CA16037596
NM_001354901.2:c.7300C>A