Allele Registry

Canonical Allele Identifier: PA3057592122

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV005279521

ClinVar Variation:

3798072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys827Glu	CA382543187 NM_001351834.2:c.2479A>G