Allele Registry

Canonical Allele Identifier: PA2741867704

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003606215

ClinVar Variation:

2814127

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp2720Glu	CA382562471 NM_001351834.2:c.8160T>A CA382562472 NM_001351834.2:c.8160T>G