Allele Registry

Canonical Allele Identifier: PA913191581

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000777628

RCV001227403

ClinVar Variation:

631417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys793Gln	CA382540996 NM_000051.4:c.2377A>C