Allele Registry

Canonical Allele Identifier: PA916035014

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000628021

ClinVar Variation:

524320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.His2981Tyr	CA382530122 NM_001351834.2:c.8941C>T