Allele Registry

Canonical Allele Identifier: PA916033364

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000165416

RCV001327802

ClinVar Variation:

185911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys1701Glu	CA193341 NM_001351834.2:c.5101A>G