Allele Registry

Canonical Allele Identifier: PA286909

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000115218

RCV000195828

RCV000589184

RCV000763707

RCV001263508

RCV001799619

RCV003237337

ClinVar Variation:

127413

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Tyr1961Cys	CA286907 NM_000051.4:c.5882A>G