Allele Registry

Canonical Allele Identifier: PA2827629045

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000164338

RCV000231502

RCV000416278

RCV001535538

RCV002288733

RCV002509264

RCV004552886

ClinVar Variation:

184988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr39Ala	CA190693 NM_001351834.2:c.115A>G