Allele Registry

Canonical Allele Identifier: PA2580206776

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003026922

ClinVar Variation:

2112642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Arg2723Gly	CA382562484 NM_001351834.2:c.8167A>G