Allele Registry

Canonical Allele Identifier: PA916034658

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000567531

ClinVar Variation:

481337

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp2721Gly	CA382562476 NM_001351834.2:c.8162A>G