Allele Registry

Canonical Allele Identifier: PA916032840

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000221928

RCV000627863

RCV001770185

ClinVar Variation:

233974

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn1273Asp	CA10579122 NM_001351834.2:c.3817A>G