Allele Registry

Canonical Allele Identifier: PA916032063

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001014548

RCV001203652

ClinVar Variation:

820773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr710Ala	CA6264953 NM_001351834.2:c.2128A>G