Allele Registry

Canonical Allele Identifier: PA645502922

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000226566

RCV000573693

ClinVar Variation:

236724

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr1609Ala	CA6265562 NM_000051.4:c.4825A>G