Allele Registry

Canonical Allele Identifier: PA166130

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000130300

RCV000466004

RCV002251433

RCV003230414

ClinVar Variation:

141686

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ala84Val	CA166128 NM_000051.4:c.251C>T