Allele Registry

Canonical Allele Identifier: PA916033279

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000456711

RCV000571141

RCV002473013

RCV003230499

ClinVar Variation:

407499

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp1637Gly	CA6265583 NM_001351834.2:c.4910A>G