Allele Registry

Canonical Allele Identifier: PA286765

Gene: ATM HGNC NCBI

ClinVar Allele:

132810

ClinVar RCV:

RCV000115158

RCV000565873

RCV000698456

RCV002288587

ClinVar Variation:

127353

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met855Thr	CA286763 NM_000051.4:c.2564T>C