Allele Registry

Canonical Allele Identifier: PA916033560

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000222325

RCV000587287

RCV000627966

RCV003469066

ClinVar Variation:

233138

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Cys1873Tyr	CA10579188 NM_001351834.2:c.5618G>A