Allele Registry

Canonical Allele Identifier: PA916031877

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000213694

RCV000821518

RCV003462480

RCV004547546

ClinVar Variation:

231883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Arg568Gly	CA10579021 NM_001351834.2:c.1702A>G