Allele Registry

Canonical Allele Identifier: PA2827628947

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000627990

RCV001017298

ClinVar Variation:

524305

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Val4Ile	CA382518937 NM_001351834.2:c.10G>A