Allele Registry

Canonical Allele Identifier: PA2741867718

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003606565

ClinVar Variation:

2837683

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile2752Phe	CA382562674 NM_001351834.2:c.8254A>T