Allele Registry

Canonical Allele Identifier: PA2580207133

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002371199

ClinVar Variation:

1764139

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gln2881Glu	CA382520965 NM_001351834.2:c.8641C>G