Allele Registry

Canonical Allele Identifier: PA658674097

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000566965

RCV000697660

ClinVar Variation:

485164

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Leu846Val	CA382543586 NM_000051.4:c.2536C>G