Allele Registry

Canonical Allele Identifier: PA2825033067

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002333104

ClinVar Variation:

1738125

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.His1380Asp	CA382529894 NM_000051.4:c.4138C>G