Allele Registry

Canonical Allele Identifier: PA165781

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000130136

RCV000416016

RCV000474473

RCV001798440

RCV002288635

ClinVar Variation:

141559

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met2667Val	CA165779 NM_000051.4:c.7999A>G