Allele Registry

Canonical Allele Identifier: PA2825031798

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001864693

RCV002246561

RCV002458667

ClinVar Variation:

1359332

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile826Val	CA382543162 NM_000051.4:c.2476A>G