Canonical Allele Identifier: PA2827966792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2765170
ClinVar RCV Id: RCV003538108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.His1094Arg
CA16028685
NM_001354898.2:c.3281A>G