Allele Registry

Canonical Allele Identifier: PA916031346

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000467265

RCV000579672

ClinVar Variation:

407585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu176Val	CA6264627 NM_001351834.2:c.526C>G