Allele Registry

Canonical Allele Identifier: PA916034269

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000003180

RCV003605602

ClinVar Variation:

3039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Glu2423Gly	CA115943 NM_001351834.2:c.7268A>G