Allele Registry

Canonical Allele Identifier: PA916032008

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000481061

RCV000627944

RCV000772636

ClinVar Variation:

419317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ile665Thr	CA16619131 NM_001351834.2:c.1994T>C