Allele Registry

Canonical Allele Identifier: PA645498696

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000480166

RCV000574196

RCV001222216

ClinVar Variation:

418756

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile238Thr	CA6264673 NM_000051.4:c.713T>C