Allele Registry

Canonical Allele Identifier: PA190674

Gene: ATM HGNC NCBI

ClinVar Allele:

183196

ClinVar RCV:

RCV000164332

RCV000476653

RCV000479991

RCV002225480

RCV002465546

RCV003467290

ClinVar Variation:

184982

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ala869Gly	CA190672 NM_000051.4:c.2606C>G