Allele Registry

Canonical Allele Identifier: PA2825034703

Gene: ATM HGNC NCBI

ClinVar Variation Id: 2715586

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ser2123Arg	CA382553219 NM_000051.4:c.6367A>C CA382553230 NM_000051.4:c.6369T>A CA382553233 NM_000051.4:c.6369T>G