Allele Registry

Canonical Allele Identifier: PA2825030341

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001303854

ClinVar Variation:

1006762

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Val182Ile	CA382527668 NM_000051.4:c.544G>A