Allele Registry

Canonical Allele Identifier: PA916032180

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000628148

RCV001190867

RCV003153765

RCV003317304

RCV004547764

ClinVar Variation:

524391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Met812Val	CA228399932 NM_001351834.2:c.2434A>G