Allele Registry

Canonical Allele Identifier: PA916032282

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001016008

ClinVar Variation:

821518

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp860Glu	CA382543939 NM_001351834.2:c.2580T>A CA382543941 NM_001351834.2:c.2580T>G