Allele Registry

Canonical Allele Identifier: PA645500716

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000218800

RCV000802874

ClinVar Variation:

233578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr761Ala	CA10579046 NM_000051.4:c.2281A>G