Allele Registry

Canonical Allele Identifier: PA2741866457

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003466618

RCV003500854

ClinVar Variation:

2679710

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Pro795Thr	CA382541033 NM_001351834.2:c.2383C>A