Allele Registry

Canonical Allele Identifier: PA916034359

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000166722

RCV000255700

RCV000509266

RCV000541770

RCV001175362

RCV001535786

RCV002247573

ClinVar Variation:

187037

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Cys2488Tyr	CA196568 NM_001351834.2:c.7463G>A