Canonical Allele Identifier: PA2828012682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2065558
ClinVar RCV Id: RCV003744826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His2394Arg
CA16037976
NM_001354905.2:c.7181A>G