Canonical Allele Identifier: PA1139730696
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 861635
ClinVar RCV Id: RCV001068201 RCV001186571 RCV003462608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2808Ala
CA15067466
NM_001351834.2:c.8423T>C