Allele Registry

Canonical Allele Identifier: PA916032491

Gene: ATM HGNC NCBI

ClinVar Allele:

398286

ClinVar RCV:

RCV000465215

RCV001018058

ClinVar Variation:

407711

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser1004Asn	CA16613394 NM_001351834.2:c.3011G>A