Allele Registry

Canonical Allele Identifier: PA2825036055

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003360986

ClinVar Variation:

2587765

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2720Val	CA382562470 NM_000051.4:c.8159A>T