Allele Registry

Canonical Allele Identifier: PA2825036054

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001322368

RCV002418967

ClinVar Variation:

1022458

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2720Gly	CA6266313 NM_000051.4:c.8159A>G