Canonical Allele Identifier: PA2580203482
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1796374
ClinVar RCV Id: RCV002441748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr939Ser
CA382545749
NM_001351834.2:c.2815A>T
CA382545755
NM_001351834.2:c.2816C>G