Allele Registry

Canonical Allele Identifier: PA645501181

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000235396

RCV000456860

RCV000562612

RCV002288935

ClinVar Variation:

246364

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile879Thr	CA6265070 NM_000051.4:c.2636T>C