Allele Registry

Canonical Allele Identifier: PA916032803

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000537394

RCV000567351

ClinVar Variation:

453486

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn1243Ser	CA382523786 NM_001351834.2:c.3728A>G