Allele Registry

Canonical Allele Identifier: PA658669227

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000555039

RCV002341236

ClinVar Variation:

453534

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys1560Glu	CA382534733 NM_000051.4:c.4678A>G