Allele Registry

Canonical Allele Identifier: PA2827629976

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV004521219

ClinVar Variation:

3232544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Phe858Cys	CA382543873 NM_001351834.2:c.2573T>G