Allele Registry

Canonical Allele Identifier: PA916032367

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000166264

RCV000695920

ClinVar Variation:

186637

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr915Ala	CA195398 NM_001351834.2:c.2743A>G