Allele Registry

Canonical Allele Identifier: PA2741867703

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003360986

ClinVar Variation:

2587765

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp2720Val	CA382562470 NM_001351834.2:c.8159A>T