Allele Registry

Canonical Allele Identifier: PA355347

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000204432

RCV000780879

RCV001180108

RCV001778793

ClinVar Variation:

219803

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile709Val	CA348661 NM_000051.4:c.2125A>G