Allele Registry

Canonical Allele Identifier: PA334657

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000168364

RCV000221360

RCV000236794

RCV003468831

ClinVar Variation:

188339

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr1871Ile	CA334655 NM_000051.4:c.5612C>T