Allele Registry

Canonical Allele Identifier: PA166863

Gene: ATM HGNC NCBI

ClinVar Allele:

151658

ClinVar RCV:

RCV000130667

RCV000167917

RCV000482225

RCV002298480

RCV003153421

ClinVar Variation:

141944

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg785His	CA166861 NM_000051.4:c.2354G>A