Allele Registry

Canonical Allele Identifier: PA916034836

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000167366

RCV000473223

RCV000779779

RCV001562843

ClinVar Variation:

187621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile2844Val	CA198113 NM_001351834.2:c.8530A>G