Canonical Allele Identifier: PA916033586
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181970
ClinVar RCV Id: RCV000159737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1893Thr
CA298284
NM_001351834.2:c.5677T>A