Allele Registry

Canonical Allele Identifier: PA298079

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000159660

RCV000464909

RCV000562069

RCV003467222

ClinVar Variation:

181897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Gln2802Arg	CA298077 NM_000051.4:c.8405A>G