Allele Registry

Canonical Allele Identifier: PA286768

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000115159

RCV000534079

RCV000580576

RCV003460801

ClinVar Variation:

127354

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp860Asn	CA286766 NM_000051.4:c.2578G>A