Allele Registry

Canonical Allele Identifier: PA916035034

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000227223

RCV000569551

RCV000590595

RCV002057232

RCV003153520

ClinVar Variation:

236795

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile2998Thr	CA6266514 NM_001351834.2:c.8993T>C