Allele Registry

Canonical Allele Identifier: PA891866363

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000528884

RCV002454712

RCV003321643

RCV003471332

ClinVar Variation:

453460

1730081

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338764.1:p.Ser111Arg	CA382521833 NM_001351835.2:c.331A>C CA382521844 NM_001351835.2:c.333T>A CA382521846 NM_001351835.2:c.333T>G