Allele Registry

Canonical Allele Identifier: PA916034500

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000546599

RCV000777212

ClinVar Variation:

453705

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Cys2607Arg	CA382561300 NM_001351834.2:c.7819T>C