Allele Registry

Canonical Allele Identifier: PA916032571

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000214272

RCV000671975

RCV001546529

RCV003153495

RCV003468979

ClinVar Variation:

229707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Met1064Val	CA6265222 NM_001351834.2:c.3190A>G