Allele Registry

Canonical Allele Identifier: PA916033355

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000131765

RCV001048603

ClinVar Variation:

142567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ala1694Gly	CA168721 NM_001351834.2:c.5081C>G