Canonical Allele Identifier: PA2580203901
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1736788
ClinVar RCV Id: RCV002375596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1332Val
CA382527409
NM_001351834.2:c.3994A>G