Allele Registry

Canonical Allele Identifier: PA916031618

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000236390

RCV001857816

ClinVar Variation:

246391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ser367Pro	CA10584321 NM_001351834.2:c.1099T>C