Allele Registry

Canonical Allele Identifier: PA2827629171

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000115169

RCV000196996

RCV000515313

RCV000588846

RCV000855626

RCV001293035

ClinVar Variation:

127364

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser99Gly	CA286794 NM_001351834.2:c.295A>G