Allele Registry

Canonical Allele Identifier: PA916034662

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000580924

ClinVar Variation:

489596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Arg2723Ser	CA382562489 NM_001351834.2:c.8169A>C CA382562490 NM_001351834.2:c.8169A>T