Canonical Allele Identifier: PA916031513
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 653484
ClinVar RCV Id: RCV000809268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His290Asn
CA382529522
NM_001351834.2:c.868C>A