Allele Registry

Canonical Allele Identifier: PA2741866675

Gene: ATM HGNC NCBI

ClinVar Allele:

2921687

ClinVar RCV:

RCV003500226

ClinVar Variation:

2760507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asn1062Thr	CA382515651 NM_001351834.2:c.3185A>C