Allele Registry

Canonical Allele Identifier: PA916031372

Gene: ATM HGNC NCBI

ClinVar Allele:

139474

ClinVar RCV:

RCV000122861

RCV000563677

ClinVar Variation:

135762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.His192Asp	CA332342 NM_001351834.2:c.574C>G