Canonical Allele Identifier: PA2828014697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg216Gly
CA012188
NM_001354903.2:c.646C>G