Allele Registry

Canonical Allele Identifier: PA916032292

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000220289

RCV001325433

ClinVar Variation:

233343

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser864Gly	CA6265064 NM_001351834.2:c.2590A>G