Allele Registry

Canonical Allele Identifier: PA916034936

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000221292

RCV000802642

RCV003316210

ClinVar Variation:

230841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp2913Tyr	CA10579315 NM_001351834.2:c.8737G>T