Allele Registry

Canonical Allele Identifier: PA2825033939

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002299310

ClinVar Variation:

1714993

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe1774Tyr	CA382543003 NM_000051.4:c.5321T>A