Allele Registry

Canonical Allele Identifier: PA2580203362

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002446225

ClinVar Variation:

1789100

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys764Glu	CA382539708 NM_001351834.2:c.2290A>G