Allele Registry

Canonical Allele Identifier: PA168164

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000131441

RCV000233331

RCV000235239

ClinVar Variation:

142359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asn562Ser	CA168162 NM_000051.4:c.1685A>G