Canonical Allele Identifier: PA916032259
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233516
ClinVar RCV Id: RCV000220649 RCV001043225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu850Gly
CA10579060
NM_001351834.2:c.2549A>G