Allele Registry

Canonical Allele Identifier: PA2825031548

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001065057

ClinVar Variation:

859042

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile709Leu	CA382538633 NM_000051.4:c.2125A>C