Allele Registry

Canonical Allele Identifier: PA916033200

Gene: ATM HGNC NCBI

ClinVar Allele:

183295

ClinVar RCV:

RCV000165250

RCV000531059

RCV002273966

RCV003468736

ClinVar Variation:

185766

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.His1568Tyr	CA192867 NM_001351834.2:c.4702C>T