Allele Registry

Canonical Allele Identifier: PA2580203363

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002296252

ClinVar Variation:

1717073

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys764Gln	CA382539714 NM_001351834.2:c.2290A>C