Allele Registry

Canonical Allele Identifier: PA916032277

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000707214

RCV001772014

RCV002458324

ClinVar Variation:

582998

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn859Ser	CA382543900 NM_001351834.2:c.2576A>G