Allele Registry

Canonical Allele Identifier: PA916032122

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000218800

RCV000802874

ClinVar Variation:

233578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr761Ala	CA10579046 NM_001351834.2:c.2281A>G