Allele Registry

Canonical Allele Identifier: PA2825036135

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001058550

RCV001760010

RCV002429677

RCV003467793

ClinVar Variation:

853689

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr2751Ser	CA382562669 NM_000051.4:c.8251A>T CA382562672 NM_000051.4:c.8252C>G