Allele Registry

Canonical Allele Identifier: PA916032065

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000129789

RCV000688954

ClinVar Variation:

141316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn711Asp	CA165093 NM_001351834.2:c.2131A>G