Allele Registry

Canonical Allele Identifier: PA2741866451

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003500256

ClinVar Variation:

2761704

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser794Thr	CA382541023 NM_001351834.2:c.2381G>C