Allele Registry

Canonical Allele Identifier: PA891844997

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000706609

RCV002422610

ClinVar Variation:

582517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr710Lys	CA382538647 NM_000051.4:c.2129C>A