Allele Registry

Canonical Allele Identifier: PA165787

Gene: ATM HGNC NCBI

ClinVar Allele:

151275

ClinVar RCV:

RCV000130139

RCV000466948

RCV000478287

RCV001196781

ClinVar Variation:

141561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr460Met	CA165785 NM_000051.4:c.1379C>T