Allele Registry

Canonical Allele Identifier: PA658745893

Gene: ATM HGNC NCBI

ClinVar Variation Id: 490724

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe2686Leu	CA382561941 NM_000051.4:c.8056T>C CA382561951 NM_000051.4:c.8058T>A CA382561952 NM_000051.4:c.8058T>G