Allele Registry

Canonical Allele Identifier: PA2825031731

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001015350

RCV003605703

ClinVar Variation:

821185

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Pro795Ala	CA382541034 NM_000051.4:c.2383C>G