Allele Registry

Canonical Allele Identifier: PA916034652

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000165327

RCV000457425

RCV001529786

RCV002247570

RCV003313782

RCV003468741

ClinVar Variation:

185832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Arg2719Cys	CA193094 NM_001351834.2:c.8155C>T