Allele Registry

Canonical Allele Identifier: PA916032285

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000775688

RCV002535547

ClinVar Variation:

630420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Tyr861His	CA382543948 NM_001351834.2:c.2581T>C