Allele Registry

Canonical Allele Identifier: PA916034659

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000628134

ClinVar Variation:

524385

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu2722_Val2727del	CA658797754 NM_001351834.2:c.8164_8181del