Allele Registry

Canonical Allele Identifier: PA1139734708

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001065057

ClinVar Variation:

859042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile709Leu	CA382538633 NM_001351834.2:c.2125A>C