Allele Registry

Canonical Allele Identifier: PA916032279

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000232136

RCV000479651

RCV000574247

RCV002503882

RCV003238746

RCV004547575

ClinVar Variation:

236692

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp860Val	CA6265063 NM_001351834.2:c.2579A>T