Allele Registry

Canonical Allele Identifier: PA2580203379

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002861552

ClinVar Variation:

2014549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn796Asp	CA382541048 NM_001351834.2:c.2386A>G