Allele Registry

Canonical Allele Identifier: PA916032696

Gene: ATM HGNC NCBI

ClinVar Allele:

460937

ClinVar RCV:

RCV000558586

RCV002341233

RCV003470667

ClinVar Variation:

453470

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser1163Tyr	CA6265299 NM_001351834.2:c.3488C>A