Allele Registry

Canonical Allele Identifier: PA2499251115

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001354781

ClinVar Variation:

1049112

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser794Cys	CA382541017 NM_001351834.2:c.2380A>T