Allele Registry

Canonical Allele Identifier: PA2825036442

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002371199

ClinVar Variation:

1764139

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Gln2881Glu	CA382520965 NM_000051.4:c.8641C>G