Allele Registry

Canonical Allele Identifier: PA1139728366

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001056386

ClinVar Variation:

851883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Val2424Glu	CA382559768 NM_001351834.2:c.7271T>A