Allele Registry

Canonical Allele Identifier: PA2825036065

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003026922

ClinVar Variation:

2112642

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg2723Gly	CA382562484 NM_000051.4:c.8167A>G