Allele Registry

Canonical Allele Identifier: PA2825031726

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001307795

ClinVar Variation:

1010202

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys793Arg	CA382541002 NM_000051.4:c.2378A>G