Allele Registry

Canonical Allele Identifier: PA916032069

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000569489

RCV000816814

ClinVar Variation:

481289

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr714Ile	CA382538703 NM_001351834.2:c.2141C>T