Allele Registry

Canonical Allele Identifier: PA2499251066

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001324911

ClinVar Variation:

1024697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys828Met	CA382543218 NM_001351834.2:c.2483A>T