Allele Registry

Canonical Allele Identifier: PA916031439

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000480166

RCV000574196

RCV001222216

ClinVar Variation:

418756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile238Thr	CA6264673 NM_001351834.2:c.713T>C