Allele Registry

Canonical Allele Identifier: PA2741866482

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003606503

ClinVar Variation:

2834021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Lys828Asn	CA382543219 NM_001351834.2:c.2484G>C CA382543220 NM_001351834.2:c.2484G>T