Allele Registry

Canonical Allele Identifier: PA645499143

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000236757

RCV000460140

RCV000565895

ClinVar Variation:

246498

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr371Ile	CA10584322 NM_000051.4:c.1112C>T