Allele Registry

Canonical Allele Identifier: PA2825036243

Gene: ATM HGNC NCBI

ClinVar Variation Id: 661938

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe2796Leu	CA382516578 NM_000051.4:c.8386T>C CA382516596 NM_000051.4:c.8388C>A CA382516601 NM_000051.4:c.8388C>G