Allele Registry

Canonical Allele Identifier: PA2825033243

Gene: ATM HGNC NCBI

ClinVar Variation Id: 1740189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe1463Leu	CA228375449 NM_000051.4:c.4387T>C CA382532165 NM_000051.4:c.4389T>A CA382532166 NM_000051.4:c.4389T>G