Allele Registry

Canonical Allele Identifier: PA916033906

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000627930

RCV002257861

ClinVar Variation:

524276

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr2113Ala	CA382552306 NM_001351834.2:c.6337A>G