Allele Registry

Canonical Allele Identifier: PA916034809

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000567443

RCV000806553

ClinVar Variation:

485207

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gln2828Glu	CA382518054 NM_001351834.2:c.8482C>G