Allele Registry

Canonical Allele Identifier: PA2825036060

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001373596

ClinVar Variation:

1063730

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2721Glu	CA382562478 NM_000051.4:c.8163C>A CA382562479 NM_000051.4:c.8163C>G