Allele Registry

Canonical Allele Identifier: PA916032358

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159702

RCV000474750

RCV000567796

RCV001711426

RCV003492638

RCV004551372

ClinVar Variation:

181936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gln912Arg	CA298188 NM_001351834.2:c.2735A>G