Allele Registry

Canonical Allele Identifier: PA658745982

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000580924

ClinVar Variation:

489596

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg2723Ser	CA382562489 NM_000051.4:c.8169A>C CA382562490 NM_000051.4:c.8169A>T