Canonical Allele Identifier: PA916031540
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 229990
ClinVar RCV Id: RCV000216322 RCV000471282 RCV000586464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile311Val
CA10578984
NM_001351834.2:c.931A>G