Allele Registry

Canonical Allele Identifier: PA916035057

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000564180

RCV001210907

ClinVar Variation:

482635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Arg3008Gly	CA382531129 NM_001351834.2:c.9022C>G