Allele Registry

Canonical Allele Identifier: PA916031853

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000230533

RCV000575956

RCV001174987

RCV001770186

RCV001798728

ClinVar Variation:

236676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr548Ala	CA10582796 NM_001351834.2:c.1642A>G