Allele Registry

Canonical Allele Identifier: PA916034704

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000569218

RCV001220325

ClinVar Variation:

481180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys2756Arg	CA382562700 NM_001351834.2:c.8267A>G