Allele Registry

Canonical Allele Identifier: PA916032281

Gene: ATM HGNC NCBI

ClinVar Allele:

475676

ClinVar RCV:

RCV000563848

RCV000627857

RCV001770508

RCV003476327

ClinVar Variation:

481130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp860Gly	CA228406449 NM_001351834.2:c.2579A>G