Allele Registry

Canonical Allele Identifier: PA916035185

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000472729

RCV000775928

ClinVar Variation:

407674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338765.1:p.Lys41Glu	CA16613044 NM_001351836.2:c.121A>G