Allele Registry

Canonical Allele Identifier: PA916033243

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000226566

RCV000573693

ClinVar Variation:

236724

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr1609Ala	CA6265562 NM_001351834.2:c.4825A>G