Allele Registry

Canonical Allele Identifier: PA169890

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000132462

RCV000168295

RCV000236226

RCV001201309

RCV001355859

RCV001798460

RCV002225449

ClinVar Variation:

142966

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met963Val	CA169888 NM_000051.4:c.2887A>G