Allele Registry

Canonical Allele Identifier: PA2741866766

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003396068

RCV003605875

ClinVar Variation:

2642358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Tyr1252Cys	CA382524253 NM_001351834.2:c.3755A>G