Allele Registry

Canonical Allele Identifier: PA169735

Gene: ATM HGNC NCBI

ClinVar Allele:

152627

ClinVar RCV:

RCV000132385

RCV000233534

RCV000236602

RCV001197402

RCV001355326

RCV002465534

ClinVar Variation:

142913

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg32Cys	CA169733 NM_000051.4:c.94C>T