Allele Registry

Canonical Allele Identifier: PA3057597643

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV005293834

ClinVar Variation:

3803211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Phe1774Val	CA382542999 NM_001351834.2:c.5320T>G