Allele Registry

Canonical Allele Identifier: PA2827944705

Gene: APC HGNC NCBI

ClinVar Variation Id: 1172116

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341824.1:p.Met1638Ile	CA16032097 NM_001354895.2:c.4914G>A CA16032098 NM_001354895.2:c.4914G>C CA16032099 NM_001354895.2:c.4914G>T