Allele Registry

Canonical Allele Identifier: PA2573202022

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001999098

ClinVar Variation:

1495049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Tyr1252Phe	CA382524261 NM_001351834.2:c.3755A>T