Allele Registry

Canonical Allele Identifier: PA916034168

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000583313

RCV003465304

ClinVar Variation:

490685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu2338Pro	CA382558722 NM_001351834.2:c.7013T>C