Allele Registry

Canonical Allele Identifier: PA2499251064

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001307795

ClinVar Variation:

1010202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys793Arg	CA382541002 NM_001351834.2:c.2378A>G