Allele Registry

Canonical Allele Identifier: PA916034148

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000115236

RCV000122881

RCV000212052

RCV001375520

RCV002477275

RCV003460809

ClinVar Variation:

127431

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ala2325Val	CA286950 NM_001351834.2:c.6974C>T