Canonical Allele Identifier: PA2828012511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His2366Arg
CA048553
NM_001354905.2:c.7097A>G