Canonical Allele Identifier: PA2828012683
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760034
ClinVar RCV Id: RCV002396452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His2394Asn
CA16037972
NM_001354905.2:c.7180C>A