Allele Registry

Canonical Allele Identifier: PA916031437

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000628113

RCV000777651

ClinVar Variation:

524373

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr237Ala	CA6264672 NM_001351834.2:c.709A>G