Allele Registry

Canonical Allele Identifier: PA645504757

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000459044

ClinVar Variation:

407586

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys2810Glu	CA16613453 NM_000051.4:c.8428A>G