Allele Registry

Canonical Allele Identifier: PA2580203361

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002446155

ClinVar Variation:

1789007

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu762Arg	CA382539687 NM_001351834.2:c.2285T>G