Allele Registry

Canonical Allele Identifier: PA916033734

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000565498

RCV001298160

ClinVar Variation:

481263

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu2006Val	CA382549810 NM_001351834.2:c.6016T>G