Allele Registry

Canonical Allele Identifier: PA916034206

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000574066

RCV001217694

ClinVar Variation:

478945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Val2367Leu	CA382559394 NM_001351834.2:c.7099G>C