Canonical Allele Identifier: PA2828031992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.His230Arg
CA048853
NM_001354904.2:c.689A>G