Allele Registry

Canonical Allele Identifier: PA298104

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159670

RCV000196967

RCV000212097

RCV000779780

RCV003153436

ClinVar Variation:

181906

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met3011Val	CA298102 NM_000051.4:c.9031A>G