Allele Registry

Canonical Allele Identifier: PA916035060

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159670

RCV000196967

RCV000212097

RCV000779780

RCV003153436

ClinVar Variation:

181906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Met3011Val	CA298102 NM_001351834.2:c.9031A>G