Allele Registry

Canonical Allele Identifier: PA3057249414

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV004573891

ClinVar Variation:

3240760

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Pro795Arg	CA382541043 NM_001351834.2:c.2384C>G