Allele Registry

Canonical Allele Identifier: PA2825031671

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV002446225

ClinVar Variation:

1789100

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys764Glu	CA382539708 NM_000051.4:c.2290A>G