Allele Registry

Canonical Allele Identifier: PA645502849

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000236361

RCV000471874

RCV000566756

RCV000780886

RCV003469180

ClinVar Variation:

245791

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Tyr1544Cys	CA6265523 NM_000051.4:c.4631A>G