Allele Registry

Canonical Allele Identifier: PA645503741

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000485190

RCV000560466

RCV001025791

ClinVar Variation:

421478

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys2303Met	CA16619222 NM_000051.4:c.6908A>T