Allele Registry

Canonical Allele Identifier: PA356097

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000206155

RCV000563514

RCV000710666

ClinVar Variation:

219746

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asn796Tyr	CA350217 NM_000051.4:c.2386A>T