Allele Registry

Canonical Allele Identifier: PA916032238

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000163825

RCV000205271

RCV000515444

RCV000589287

RCV003492681

ClinVar Variation:

184552

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp841Ala	CA189280 NM_001351834.2:c.2522A>C