Canonical Allele Identifier: PA916042160
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg226Gly
CA012188
NM_001354902.2:c.676C>G