Allele Registry

Canonical Allele Identifier: PA356409

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000206792

RCV000222064

RCV002243888

RCV003493501

ClinVar Variation:

220354

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile709Met	CA350788 NM_000051.4:c.2127T>G