Allele Registry

Canonical Allele Identifier: PA298224

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159715

RCV000211998

RCV000335065

RCV003226222

ClinVar Variation:

181948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr1118Ala	CA298222 NM_000051.4:c.3352A>G