Allele Registry

Canonical Allele Identifier: PA2499251040

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001318045

ClinVar Variation:

1018705

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu2722Arg	CA382562483 NM_001351834.2:c.8165T>G