Canonical Allele Identifier: PA2828019702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2765170
ClinVar RCV Id: RCV003538108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His1018Arg
CA16028685
NM_001354903.2:c.3053A>G