Allele Registry

Canonical Allele Identifier: PA916034651

Gene: ATM HGNC NCBI

ClinVar Allele:

398364

ClinVar RCV:

RCV000463539

ClinVar Variation:

407703

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gly2718Ser	CA16613449 NM_001351834.2:c.8152G>A